Laboratory for Molecular and Functional Imaging: from Physiology to Therapy, UMR 5231 CNRS/University Victor Segalen Bordeaux, 146 rue Leo Saignat, Case 117, 33076 Bordeaux, France.
Contrast Media Mol Imaging. 2011 Jul-Aug;6(4):267-74. doi: 10.1002/cmmi.426. Epub 2010 Dec 29.
Many potent anti-cancer drugs have an intracellular mode of action, but are limited in crossing the cell membrane, resulting in a reduced clinical efficacy. Ultrasound (US) is known to facilitate the penetration of drugs into tumors cells. However (molecular) imaging techniques that monitor in vivo the underlying processes of US-triggered drug delivery are lacking. The objective of this study was to demonstrate the feasibility of using a fluorescent nuclear acid stain (TOTO-3) as a model drug to monitor in real-time US-mediated delivery by in vivo fluorescence imaging. Following co-injection of TOTO-3 and microbubbles US was applied to the tumor. The time course of the drug delivery process was monitored by fluorescence imaging. Immunohistological analysis and in vitro experiments were performed to investigate the results in more detail. A significant signal intensity enhancement of the US-treated tumor was observed that indicates intracellular delivery of the dye. In the control tumor TOTO-3 signal was strongly associated with macrophages, which was not the case for the sonicated tumor. The capability of macrophages to uptake TOTO-3 was confirmed in vitro. This study demonstrates that an optical contrast agent with similar characteristics to an anti-cancer drug may be used for continuous in vivo monitoring of the drug delivery process.
许多有效的抗癌药物具有细胞内作用模式,但它们穿过细胞膜的能力有限,导致临床疗效降低。已知超声 (US) 可促进药物进入肿瘤细胞。然而,缺乏监测 US 触发药物输送的体内潜在过程的(分子)成像技术。本研究的目的是证明使用荧光核酸染料(TOTO-3)作为模型药物通过体内荧光成像实时监测 US 介导的递药的可行性。在 TOTO-3 和微泡共同注射后,将 US 应用于肿瘤。通过荧光成像监测药物输送过程的时间过程。进行免疫组织化学分析和体外实验以更详细地研究结果。观察到 US 处理的肿瘤的信号强度显著增强,表明染料的细胞内递药。在对照肿瘤中,TOTO-3 信号与巨噬细胞强烈相关,而在超声处理的肿瘤中则不是这种情况。体外实验证实了巨噬细胞摄取 TOTO-3 的能力。这项研究表明,具有类似于抗癌药物特征的光学造影剂可用于连续体内监测药物输送过程。